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Sustained-release and instant-release verapamil in treatment of angina pectoris.

Abstract
The efficacy of a sustained-release preparation of verapamil (verapamil-SR) has been compared with that of a conventional instant-release formulation (verapamil-IR) in 10 patients with stable angina pectoris treated for 3 weeks with both preparations. The diurnal serum concentrations of verapamil and norverapamil did not differ significantly during treatment with verapamil-IR 120 mg t.i.d. and verapamil-SR 360 mg once daily, but verapamil-SR 240 mg produced significantly lower serum concentrations. The differences did not affect the exercise capacity or the occurrence of ST-segment depression during maximal exercise. Verapamil-SR was well tolerated. A multiple instant-release dosage regime can now be replaced by once daily administration of the sustained-release preparation.
AuthorsC M Jespersen, N A Klitgaard, H Nielsen, J F Hansen
JournalEuropean journal of clinical pharmacology (Eur J Clin Pharmacol) Vol. 36 Issue 6 Pg. 625-7 ( 1989) ISSN: 0031-6970 [Print] Germany
PMID2776821 (Publication Type: Clinical Trial, Controlled Clinical Trial, Journal Article, Randomized Controlled Trial)
Chemical References
  • Delayed-Action Preparations
  • norverapamil
  • Verapamil
Topics
  • Angina Pectoris (drug therapy)
  • Delayed-Action Preparations
  • Double-Blind Method
  • Electrocardiography
  • Exercise Test
  • Female
  • Hemodynamics
  • Humans
  • Male
  • Verapamil (administration & dosage, analogs & derivatives, blood, therapeutic use)

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